Associate Director, Manufacturing

The Associate Director, Manufacturing will lead oversight of commercial contract manufacturing organizations and other third‑party suppliers for a pharmaceutical‑biotechnology company, ensuring that processes transferred from R&D to commercial partners meet schedule, inventory and profitability goals. The role involves building and maintaining strong relationships with CMOs, negotiating contracts, creating SOPs, and guiding teams that monitor supplier performance through metrics and regular communication. Day‑to‑day duties include selecting and qualifying CMOs, diagnosing and resolving process issues, and collaborating with Quality, Regulatory Affairs and other functions to address deviations, support filings and prepare for inspections. The incumbent will develop timelines and deliverables for API manufacturing, optimize processes for quality and cost efficiency, and provide on‑site coverage when needed, while also supervising, training and mentoring staff. Candidates must hold a BS in Engineering or Chemistry (or an equivalent mix of education and experience), with a master’s or Ph.D. preferred, and bring at least ten years of progressive experience in the pharma/biotech sector, including six years in a leadership capacity. Required expertise covers contract service provider management, deep understanding of biopharmaceutical development, regulatory filings and GMP change regulations, and the ability to travel frequently to manufacturing sites across the EU and Asia. The position offers exposure to strategic planning with senior leadership, involvement in complex cross‑functional projects, and a travel schedule that can reach 50 % of the time, both domestically and internationally. The role also includes on‑site process responsibility and the opportunity to influence manufacturing strategy across a global network.